This paragraph should settle a few arguments:
"End of trial activities for all three clinical trials are primarily in the hands of external Contract ResearchOrganisations (CROs) that are responsible for independent management and oversight of all data generatedthroughout clinical trials. Once all post-trial activities are completed, the trial database will be locked, the dataunblinded and statistical analyses of the data can be completed"
Ann: Half Yearly Report and Accounts, page-4
-
- There are more pages in this discussion • 144 more messages in this thread...
You’re viewing a single post only. To view the entire thread just sign in or Join Now (FREE)
